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Relevant bibliographies by topics / Ultrafast solvation dynamics

Academic literature on the topic 'Ultrafast solvation dynamics'

Author: Grafiati

Published: 6 September 2023

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Journal articles on the topic "Ultrafast solvation dynamics"

1

Zolotov, B., D. Huppert, and B. D. Fainberg. "Quantum beats and ultrafast solvation dynamics." Journal of Chemical Physics 111, no. 14 (October 8, 1999): 6510–20. http://dx.doi.org/10.1063/1.480027.

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2

Cao, Simin, Haoyang Li, Zenan Zhao, Sanjun Zhang, Jinquan Chen, Jianhua Xu, Jay R. Knutson, and Ludwig Brand. "Ultrafast Fluorescence Spectroscopy via Upconversion and Its Applications in Biophysics." Molecules 26, no. 1 (January 3, 2021): 211. http://dx.doi.org/10.3390/molecules26010211.

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In this review, the experimental set-up and functional characteristics of single-wavelength and broad-band femtosecond upconversion spectrophotofluorometers developed in our laboratory are described. We discuss applications of this technique to biophysical problems, such as ultrafast fluorescence quenching and solvation dynamics of tryptophan, peptides, proteins, reduced nicotinamide adenine dinucleotide (NADH), and nucleic acids. In the tryptophan dynamics field, especially for proteins, two types of solvation dynamics on different time scales have been well explored: ~1 ps for bulk water, and tens of picoseconds for “biological water”, a term that combines effects of water and macromolecule dynamics. In addition, some proteins also show quasi-static self-quenching (QSSQ) phenomena. Interestingly, in our more recent work, we also find that similar mixtures of quenching and solvation dynamics occur for the metabolic cofactor NADH. In this review, we add a brief overview of the emerging development of fluorescent RNA aptamers and their potential application to live cell imaging, while noting how ultrafast measurement may speed their optimization.

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3

Perera, Lalith, and Max L. Berkowitz. "Ultrafast solvation dynamics in a Stockmayer fluid." Journal of Chemical Physics 97, no. 7 (October 1992): 5253–54. http://dx.doi.org/10.1063/1.463826.

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4

Jiao, Yishuo, Bernhard Adams, and Christoph Rose-Petruck. "Ultrafast X-ray measurements of the glass-like, high-frequency stiffness of aqueous solutions." Physical Chemistry Chemical Physics 19, no. 31 (2017): 21095–100. http://dx.doi.org/10.1039/c7cp02747h.

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The ultrafast dynamics of the domains surrounding solutes in aqueous solution were measured using laser-generating GHz phonons in 30 mM ferrocyanide solutions and the resulting molecular motions of the solutes and their hydrogen-bonded solvation shells were detected using ultrafast X-ray absorption spectroscopy (UXAS).

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Nome, René A. "Ultrafast dynamics of solvation: the story so far." Journal of the Brazilian Chemical Society 21, no. 12 (December 2010): 2189–204. http://dx.doi.org/10.1590/s0103-50532010001200005.

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Ma, Jangseok, David Vanden Bout, and Mark Berg. "Solvation dynamics studied by ultrafast transient hole burning." Journal of Molecular Liquids 65-66 (November 1995): 301–4. http://dx.doi.org/10.1016/0167-7322(95)00821-x.

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7

Cota, Roberto, Ambuj Tiwari, Bernd Ensing, Huib J. Bakker, and Sander Woutersen. "Hydration interactions beyond the first solvation shell in aqueous phenolate solution." Physical Chemistry Chemical Physics 22, no. 35 (2020): 19940–47. http://dx.doi.org/10.1039/d0cp01209b.

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Niu, Xinmiao, Prabhat Gautam, Zhuoran Kuang, Craig P. Yu, Yuanyuan Guo, Hongwei Song, Qianjin Guo, Julian M. W. Chan, and Andong Xia. "Intramolecular charge transfer and solvation dynamics of push–pull dyes with different π-conjugated linkers." Physical Chemistry Chemical Physics 21, no. 31 (2019): 17323–31. http://dx.doi.org/10.1039/c9cp02559f.

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The solvation-dependent excited state dynamics of two push–pull fluorophores with donor–π–acceptor (D–π–A) structures were investigated using steady-state and ultrafast transient absorption (TA) spectroscopy, backed by theoretical calculations.

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9

Roy, Srabani, and Biman Bagchi. "Ultrafast underdamped solvation: Agreement between computer simulation and various theories of solvation dynamics." Journal of Chemical Physics 99, no. 2 (July 15, 1993): 1310–19. http://dx.doi.org/10.1063/1.465375.

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de Boeij, Wim P., Maxim S. Pshenichnikov, and Douwe A. Wiersma. "ULTRAFAST SOLVATION DYNAMICS EXPLORED BY FEMTOSECOND PHOTON ECHO SPECTROSCOPIES." Annual Review of Physical Chemistry 49, no. 1 (October 1998): 99–123. http://dx.doi.org/10.1146/annurev.physchem.49.1.99.

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Dissertations / Theses on the topic "Ultrafast solvation dynamics"

1

Yang, Jin. "Ultrafast Protein Hydration Dynamics and Water-Protein Interactions." The Ohio State University, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=osu1480668103383892.

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Craigo, Kevin Alan. "Ultrafast Spectroscopic Study of Hydration and Conformational Dynamics in Calmodulin." The Ohio State University, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=osu1311089745.

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3

Chong, Sing Hwa Zewail Ahmed H. Zewail Ahmed H. "Ultrafast dynamics of barrier crossing : step-wise solvation effect on isomerization of trans-stilbene in alkane clusters /." Diss., Pasadena, Calif. : California Institute of Technology, 2001. http://resolver.caltech.edu/CaltechETD:etd-04072008-151825.

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Qin, Yangzhong. "Ultrafast Hydration Dynamics Probed by Tryptophan at Protein Surface and Protein-DNA Interface." The Ohio State University, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=osu1416998263.

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5

Cavanagh, Molly Christine. "Using the ultrafast pump-probe spectroscopy of atomic anions and the solvated electron to probe solvent structure and solvation dynamics." Diss., Restricted to subscribing institutions, 2008. http://proquest.umi.com/pqdweb?did=1581642021&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.

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Wang, Jin. "Ultrafast studies of reactive intermediates." Columbus, Ohio : Ohio State University, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1196155202.

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7

Seidel, Marco Thomas. "Solvatationsdynamik an biologischen Grenzschichten." Doctoral thesis, [S.l.] : [s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=969974124.

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8

Hydutsky, Darren P. "Ultrafast dynamics of solvation and isotope effects in dissociative processes." 2007. http://etda.libraries.psu.edu/theses/approved/WorldWideIndex/ETD-1932/index.html.

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9

Sanders, Headley Lindsay Elizabeth. "Ultrafast solvation dynamics in room temperature ionic liquids and protein environments /." 2006.

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10

Book, Lewis D. "Ultrafast dephasing of excitons in solution and photosynthetic aggregates /." 2000. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:9965060.

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Books on the topic "Ultrafast solvation dynamics"

1

Yann, Gauduel, and Rossky Peter J, eds. Ultrafast reaction dynamics and solvent effects: Royaumont, France 1993. New York: American Institute of Physics, 1994.

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2

Ultrafast solvent dynamics and nonlinear spectroscopy. 1993.

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3

(Editor), Y. Gauduel, and P. J. Rossky (Editor), eds. Ultrafast Reaction Dynamics and Solvent Effects: Proceedings of the international Research Workshop, France, August 1993 (AIP Conference Proceedings). American Institute of Physics, 1998.

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Book chapters on the topic "Ultrafast solvation dynamics"

1

Fleming, G. R., and M. P. Maroncelli. "Dynamics of Polar Solvation." In Ultrafast Phenomena VI, 532–36. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-83644-2_149.

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2

Neria, E., and A. Nitzan. "Adiabatic and Nonadiabatic Effects in Solvation Dynamics." In Ultrafast Phenomena VIII, 618–20. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84910-7_199.

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3

Kropman, Michel F., Han-Kwang Nienhuys, and Huib J. Bakker. "Dynamics of water in ionic solvation shells." In Ultrafast Phenomena XIII, 429–31. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-642-59319-2_133.

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4

Barbara, Paul F., Tai Jong Kang, Włodzimięrz Jarzeba, and Teresa Fonseca. "Solvation Dynamics and Ultrafast Electron Transfer." In The Jerusalem Symposia on Quantum Chemistry and Biochemistry, 273–92. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0489-7_21.

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5

Zolotov, B., D. Huppert, and B. D. Fainberg. "Ultrafast solvation dynamics and quantum beats." In Springer Series in Chemical Physics, 544–46. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-72289-9_163.

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6

Hynes, James T. "Charge Transfer Reactions and Solvation Dynamics." In Ultrafast Dynamics of Chemical Systems, 345–81. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0916-1_13.

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7

Lin, Y., and C. D. Jonah. "The Dynamics of Anion Solvation in Alcohols." In Ultrafast Dynamics of Chemical Systems, 137–62. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0916-1_4.

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8

Hybl, John D., Allison W. Albrecht, and David M. Jonas. "Time dependent 2D Fourier transform spectra reveal femtosecond solvation dynamics." In Ultrafast Phenomena XII, 519–21. Berlin, Heidelberg: Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/978-3-642-56546-5_152.

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9

Syage, Jack A. "Chemistry in Clusters: Solvation at the Single Molecule Level." In Ultrafast Dynamics of Chemical Systems, 289–326. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0916-1_11.

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10

Mukamel, S., and Yi Jing Yan. "Unified Theory of Solvation Dynamics in Nonlinear Optical Processes and Electron Transfer." In Ultrafast Phenomena VI, 542–44. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-83644-2_151.

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Conference papers on the topic "Ultrafast solvation dynamics"

1

Neria, Eyal, and Abraham Nitzan. "Adiabatic and Non-Adiabatic Effects in Solvation Dynamics." In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/up.1992.tub5.

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The solvation process may in principle involve more then one adiabatic state. This is referred to as non adiabatic solvation. Adiabatic solvation proceeds on a single electronic potential surface. We study the adiabatic solvation of an ion in a polar solvent using classical molecular dynamics simulations1 concentrating on the role of the rotational and translational motion of the solvent and the contribution of the different solvation shells to the solvation process. We also present results for ion solvation dynamics in a salt solution. The non adiabatic solvation of the hydrated electron is investigated using a newly proposed method for simulating non adiabatic transitions2

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2

Rips, Ilya. "Two aspects of the solvation dynamics." In Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45388.

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3

Maroncelli, M., E. W. Castner, S. P. Webb, and G. R. Fleming. "Solvation Dynamics in Polar Liquids: Experiment and Simulation." In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1986. http://dx.doi.org/10.1364/up.1986.tha5.

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Current theoretical studies by a number of workers have focussed attention on the importance of solvation dynamics in determining the rates of reactions in solution1. This is especially true of reactions involving substantial charge redistribution in the reaction coordinate in polar solvents, where solvation energies may be quite large. The first step in testing these ideas is to obtain direct, microscopic measures of the kinetics of dipolar solvation. Experimentally, such information is available by monitoring the temporal evolution of the electronic spectrum of a probe solute after instantaneously changing its charge or dipole moment. Spectral shifts as a function of time directly monitor the course of solvation as the system reequilibrates to the new solute charge distribution.

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4

Fourkas, John T., Andrea Benigno, Jangseok Ma, David Vanden Bout, and Mark Berg. "Mechanical relaxation and solvation dynamics in nonpolar solutions." In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/up.1994.me.3.

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We have used transient hole burning measurements to make the first measurements of solvation dynamics in a completely nonpolar system: dimethyl-s-tetrazine (DMST) in n-butylbenzene.1,2 A new model for solvation based on the mechanical response of a viscoelastic solvent explains the main experimental features and predicts new features on the femtosecond timescale. Although the mechanical solvation mechanism is most prominent in nonpolar systems, it should play a role in all solvation3,4 and electronic dephasing5–8 processes.

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5

Kropman, Michel F., Han-Kwang Nienhuys, and Huib J. Bakker. "Dynamics of water in ionic solvation shells." In International Conference on Ultrafast Phenomena. Washington, D.C.: OSA, 2002. http://dx.doi.org/10.1364/up.2002.md7.

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6

Fainberg, B. D., B. Zolotov, A. Gan, and D. Huppert. "Ultrafast Spectroscopy of Solvation Dynamics: from Linear to Nonlinear Solvation Study." In EQEC'96. 1996 European Quantum Electronic Conference. IEEE, 1996. http://dx.doi.org/10.1109/eqec.1996.561894.

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7

Neria, Eyal, and Abraham Nitzan. "Numerical studies of solvation dynamics in electrolyte solutions." In Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45391.

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8

Yoshihara, Keitaro, Haridas Pal, Hideaki Shirota, Yutaka Nagasawa, and Keisuke Tominaga. "Ultrafast Dynamics in Intermolecular Electron Transfer." In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/up.1996.tha.6.

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Electron Transfer (ET) is one of the most common reactions in chemistry and biology. For the past decade critical comparison between theory1,2 and experiments3-6 has been giving important insight into the dynamical aspects of ET in solution. Contemporary ET theories which are based only upon the solvent polarization relaxation have predicted that the ET reactions are controlled by the solvent fluctuations and the maximum ET rate for a barriers reaction cannot exceed the solvation rates. The dependence of the ET rate constants on the solvation times has experimentally been demonstrated by many authors.

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9

Barbara, Paul F. "Ultrafast studies on intramolecular charge transfer and solvation dynamics." In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1990. http://dx.doi.org/10.1364/up.1990.tub2.

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Much of the recent activity on the study of fast charge (electron) transfer ET reactions stems from the growing appreciation that the rates of ET can be affected by solvent dynamics in contrast to traditional theories of ET which are based on a quasi—equilibrium assumption. Our work has emphasized femtosecond studies of the excited state, S1 small barrier, ultrafast ET reactions of aromatics, including BA, ADMA, derivatives of ADMA, and several other molecules. We have shown theoretically that emission dynamics at the short wavelength edge of the fluorescence band accurately measures the decay of the prepared (reactant’s) concentration. Results on the solvent dependence of <τET> demonstrate that the ET kinetics of the various molecules are controlled by solvation dynamics, see Table 1. However, we have shown that simple continuum models for solvation dynamics (when combined with theories of ET) do not correctly predict ET rates. Rips and Jortner have analyzed our data and shown that the MSA model (combined with ET theory) more accurately agrees with experiments. This emphasizes the importance of molecular interactions in dynamic solvent effects on chemical reactions.

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10

Bagchi, B., A. Chandra, and G. R. Fleming. "Solvation and Barrierless Electron Transfer : How Different Are the Dynamics?" In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1990. http://dx.doi.org/10.1364/up.1990.mc26.

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Dynamic polar solvent effects on barrierless electron transfer reactions have been a subject of several detailed experimental studies in the recent years1. These studies have revealed a clear connection between dynamics of electron transfer from a locally excited (LE) state and the dynamics of solvation of the newly formed charge transfer state.

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